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The Concentrations of Calcium Buffering Proteins in Mammalian Cochlear Hair Cells
Open accessAbstract
Calcium buffers are important for shaping and localizing cytoplasmic Ca 2+ transients in neurons. We measured the concentrations of the four main calcium-buffering proteins (calbindin-D28k, calretinin, parvalbumin-α, and parvalbumin-β) in rat cochlear hair cells in which Ca 2+ signaling is a central element of fast transduction and synaptic transmission. The proteins were quantified by calibrating immunogold tissue counts against gels containing known amounts of each protein, and the method was verified by application to Purkinje cells in which independent estimates exist for some of the protein concentrations. The results showed that, in animals with fully developed hearing, inner hair cells had \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(\frac{1}{10}\) \end{document} of the proteinaceous calcium buffer of outer hair cells in which the cell body contained parvalbumin-β (oncomodulin) and calbindin-D28k at levels equivalent to 5 m m calcium-binding sites. Both proteins were partially excluded from the hair bundles, which may permit fast unbuffered Ca 2+ regulation of the mechanotransducer channels. The sum of the calcium buffer concentrations decreased in inner hair cells and increased in outer hair cells as the cells developed their adult properties during cochlear maturation. The results suggest that Ca 2+ has distinct roles in the two types of hair cell, reflecting their different functions in auditory transduction. Ca 2+ is used in inner hair cells primarily for fast phase-locked synaptic transmission, whereas Ca 2+ may be involved in regulating the motor capability underlying cochlear amplification of the outer hair cell. The high concentration of calcium buffer in outer hair cells, similar only to skeletal muscle, may protect against deleterious consequences of Ca 2+ loading after acoustic overstimulation.
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Cited by
Nanodomain coupling between Ca2+ channels and sensors of exocytosis at fast mammalian synapses
Eggermann, E., Bucurenciu, I., Goswami, S. P., & Jonas, P. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3125 · Cited by 500
The Physiology of Mechanoelectrical Transduction Channels in Hearing
Fettiplace, R., & Kim, K. X. (2014) · Physiological Reviews · doi:10.1152/physrev.00038.2013 · Cited by 313
Self-citationPrestin-Driven Cochlear Amplification Is Not Limited by the Outer Hair Cell Membrane Time Constant
Johnson, S. L., Beurg, M., Marcotti, W., & Fettiplace, R. (2011) · Neuron · doi:10.1016/j.neuron.2011.04.024 · Cited by 289
Self-citationSantiago, A. N., Lim, K. Y., Opendak, M., Sullivan, R. M., & Aoki, C. (2018) · Journal of Comparative Neurology · doi:10.1002/cne.24522 · Cited by 87
Chen, G., Racay, P., Bichet, S., Celio, M. R., Eggli, P., & Schwaller, B. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.06.008 · Cited by 47
Metadata
- Authors
- Hackney, C. M., Mahendrasingam, S., Penn, A., & Fettiplace, R.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2005-08-24
- Volume
- 25
- Issue
- 34
- Pages
- 7867-7875
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- OpenAlex
- W2056149017
- Cited by
- 204
- References
- 0
- FWCI
- 4.91
- Type
- journal article
- Language
- en
- Open access
- hybrid
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- Hackney, C. M., Mahendrasingam, S., Penn, A., & Fettiplace, R. (2005). The Concentrations of Calcium Buffering Proteins in Mammalian Cochlear Hair Cells. The Journal of Neuroscience. https://doi.org/10.1523/jneurosci.1196-05.2005
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